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Provider Coaching for MAT in Opioid Use Disorder
N/A
Waitlist Available
Led By Faye Taxman, PhD
Research Sponsored by University of Wisconsin, Madison
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Site must have the funds to pay for medications for the duration of the study (24 months) from grants, insurance, or private pay
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months, 24 months
Awards & highlights
Study Summary
This trial will explore whether adding coaching and support to providers who offer medication assisted treatment (MAT) to justice-involved populations will help more people access this life-saving care.
Who is the study for?
This trial is for healthcare providers in jail/community settings who are committed to using or increasing the use of medication-assisted treatment (MAT) for individuals with opioid use disorder. Participants must have leadership support, agree to share data, and secure funds to cover medication costs for two years.Check my eligibility
What is being tested?
The study is examining the effectiveness of two evidence-based practices—NIATx Coaching and ECHO—to enhance MAT usage among justice-involved populations. It aims to foster better implementation strategies within participating sites.See study design
What are the potential side effects?
Since this trial focuses on implementation practices rather than direct medical interventions, it does not involve side effects in the traditional sense. However, there may be indirect impacts on patient care that will be monitored.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My treatment costs are covered for 24 months by insurance, grants, or out-of-pocket.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months, 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months, 24 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Number of Prescribers using MOUD
Percent of Eligible Justice Involved Persons initiated and on MOUD
Secondary outcome measures
Percent of sites that continue to use MOUD post intervention
Other outcome measures
NIATx Fidelity
Trial Design
4Treatment groups
Experimental Treatment
Group I: Low-Dose NIATx Coaching & No ECHOExperimental Treatment1 Intervention
Attend an in-person Kick-Off Meeting with Study Team & Coaches
One-hour conference call with Executive Sponsor
Two-hour NIATx webinar training with Change Leader/Team
Three (one-hour) coaching calls at months 4, 8, and 12 with Change Leader/Team
Group II: Low-Dose NIATx Coaching & ECHOExperimental Treatment2 Interventions
Attend an in-person Kick-Off Meeting with Study Team & Coaches
One-hour conference call with Executive Sponsor
Two-hour NIATx webinar training with Change Leader/Team
Three (one-hour) coaching calls at months 4, 8, and 12 with Change Leader/Team
Prescribers participate in 12 monthly (one-hour) ECHO video conference calls
Group III: High-Dose NIATx Coaching & No ECHOExperimental Treatment1 Intervention
Attend an in-person Kick-Off Meeting with Study Team & Coaches
4-hour onsite visit
11 monthly (one-hour) NIATx coaching calls
Group IV: High-Dose NIATx Coaching & ECHOExperimental Treatment2 Interventions
Attend an in-person Kick-Off Meeting with Study Team & Coaches
4-hour onsite visit (NIATx Training)
11 monthly (one-hour) NIATx coaching calls
Prescribers participate in 12 monthly (one-hour) ECHO video conference calls
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
ECHO
2022
N/A
~160
Find a Location
Who is running the clinical trial?
University of Wisconsin, MadisonLead Sponsor
1,182 Previous Clinical Trials
3,167,123 Total Patients Enrolled
George Mason UniversityOTHER
58 Previous Clinical Trials
48,530 Total Patients Enrolled
National Institute on Drug Abuse (NIDA)NIH
2,464 Previous Clinical Trials
2,618,329 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My treatment costs are covered for 24 months by insurance, grants, or out-of-pocket.My treatment site offers at least one type of medication.N/A
Research Study Groups:
This trial has the following groups:- Group 1: High-Dose NIATx Coaching & ECHO
- Group 2: Low-Dose NIATx Coaching & No ECHO
- Group 3: High-Dose NIATx Coaching & No ECHO
- Group 4: Low-Dose NIATx Coaching & ECHO
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What is the total participant count in this clinical endeavor?
"Affirmative. Clinicaltrials.gov records reveal that this clinical trial began recruiting on July 30th, 2020 and has since been updated to include 300 subjects from 1 location."
Answered by AI
Is recruitment still underway for this clinical trial?
"Affirmative. The clinicaltrials.gov website indicates that this trial, which commenced on July 30th 2020, is actively searching for participants. 300 individuals need to be recruited from a single location."
Answered by AI
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